Polymerase Chain Reaction (Latest Articles)

Latest indexed articles for 'Polymerase Chain Reaction'

Articles 1 to 10 of 200:

Association of HPV16 E6 variants with diagnostic severity in cervical cytology samples of 354 women in a US population.

29 Nov 2009 It has been suggested that DNA sequence variants of HPV16 contribute to differences in the behavior of individual cervical lesions. To address this question, we have analyzed the association of HPV16 variants with diagnostic severity in 354 ...
rec_pub_19569178-association-hpv16-e6-variants-diagnostic-severity-cervical-cytology.htm

Toward understanding the function of the universally conserved GTPase HflX from Escherichia coli: a kinetic approach.

15 Nov 2009 Protein synthesis is a highly conserved process in all living cells involving several members of the translation factor (TRAFAC) class of P-loop GTPases, which play essential roles during translation. The universally conserved GTPase HflX has ...
rec_pub_19824612-toward-understanding-function-universally-conserved-gtpase-hflx.htm

Submicroscopic infection in Plasmodium falciparum-endemic populations: a systematic review and meta-analysis.

13 Nov 2009 INTRODUCTION: Light microscopy examination of blood slides is the main method of detecting malaria infection; however, it has limited sensitivity. Low-density infections are most likely to be missed, but they contribute to the infectious reservoir. ...
rec_pub_19848588-submicroscopic-infection-plasmodium-falciparum-endemic-populations.htm

Carbonic anhydrase IX and human papillomavirus as diagnostic biomarkers of cervical dysplasia/neoplasia in women with a cytologic diagnosis of atypical glandular cells: a Gynecologic Oncology Group study in United States.

13 Nov 2009 High-risk human papillomavirus (H-HPV) infection is strongly linked to cervical neoplasia, but its role in detecting glandular lesions (GLs) is unclear. In the cervix, carbonic anhydrase IX (CA-IX) is expressed in cervical neoplasia, but rarely in ...
rec_pub_19670419-carbonic-anhydrase-ix-human-papillomavirus-diagnostic-biomarkers.htm

The potential impact of human papillomavirus vaccination in contemporary cytologically screened populations may be underestimated: an observational retrospective analysis of invasive cervical cancers.

13 Nov 2009 The aim of this study was to determine the proportion of invasive cervical cancers attributable to human papillomavirus (HPV) types 16 and 18 in a contemporary, cytologically well-screened UK population. This was achieved in a retrospective ...
rec_pub_19585507-the-potential-impact-human-papillomavirus-vaccination-contemporary.htm

Absence of IDH2 codon 172 mutation in common human cancers.

13 Nov 2009
rec_pub_19530255-absence-idh2-codon-172-mutation-common-human-cancers.htm

Detection of epidermal growth factor receptor mutations in plasma by mutant-enriched PCR assay for prediction of the response to gefitinib in patients with non-small-cell lung cancer.

13 Nov 2009 The high frequency of epidermal growth factor receptor (EGFR) mutations in tyrosine kinase inhibitor-responsive non-small-cell lung cancer (NSCLC) cases is now well established, highlighting the predictive value of activating EGFR mutations in ...
rec_pub_19530244-detection-epidermal-growth-factor-receptor-mutations-plasma-mutant.htm

Requirement of a unique Ca(2+)-binding loop for folding of Tk-subtilisin from a hyperthermophilic archaeon.

8 Nov 2009 Tk-subtilisin from the hyperthermophiolic archaeon Thermococcus kodakaraensis matures from Pro-Tk-subtilisin upon autoprocessing and degradation of Tk-propeptide [Tanaka, S., Saito, K., Chon, H., Matsumura, H., Koga, Y., Takano, K., and Kanaya, S. ...
rec_pub_19813760-requirement-unique-ca-2-binding-loop-folding-tk-subtilisin.htm

Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.

30 Oct 2009 OBJECTIVE: To report a 3-generation white family clinically diagnosed variably with Wagner, Stickler, and Jansen syndromes and screened for sequence variants in the COL2A1 and CSPG2 genes. Wagner syndrome is an autosomal dominant vitreoretinopathy ...
rec_pub_19901218-mutational-hot-spot-potential-novel-base-pair-mutation-cspg2-gene.htm

Common CCR 5 polymorphism in stroke: the CCR 5 delta32 polymorphism differentiates cardioembolism from other aetiologies of ischaemic cerebrovascular diseases.

30 Oct 2009 Inflammation is involved in the development of atherosclerosis. The CC chemokine receptor 5 (CCR5) initiates chemotaxis and modulates the inflammation secondary to atherosclerosis and related vascular diseases. The CCR5 Delta32 polymorphism ...
rec_pub_19874552-common-ccr-5-polymorphism-stroke-ccr-5-delta32-polymorphism.htm

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